Fernández JM - Search Results

1

Muscle involvement in cholesterol ester storage disease.

Navarro C, Fernández JM, Domínguez C, Ortega A, Sancho S, García J. Navarro C, et al. Among authors: fernandez jm. Neurology. 1992 May;42(5):1120-1. doi: 10.1212/wnl.42.5.1120. Neurology. 1992. PMID: 1579241 No abstract available.

2

Skin biopsy findings in glycogenosis III: clinical, biochemical, and electrophysiological correlations.

Sancho S, Navarro C, Fernández JM, Domínguez C, Ortega A, Roig M, Cervera C. Sancho S, et al. Among authors: fernandez jm. Ann Neurol. 1990 May;27(5):480-6. doi: 10.1002/ana.410270505. Ann Neurol. 1990. PMID: 2360788

3

Muscle biopsy findings in systemic capillary leak syndrome.

Navarro C, García-Bragado F, Lima J, Fernández JM. Navarro C, et al. Among authors: fernandez jm. Hum Pathol. 1990 Mar;21(3):297-301. doi: 10.1016/0046-8177(90)90230-3. Hum Pathol. 1990. PMID: 2179110

4

Peripheral neuropathy in essential mixed cryoglobulinemia.

Garcia-Bragado F, Fernandez JM, Navarro C, Villar M, Bonaventura I. Garcia-Bragado F, et al. Among authors: fernandez jm. Arch Neurol. 1988 Nov;45(11):1210-4. doi: 10.1001/archneur.1988.00520350048015. Arch Neurol. 1988. PMID: 2847694

5

Late juvenile metachromatic leukodystrophy treated with bone marrow transplantation; a 4-year follow-up study.

Navarro C, Fernández JM, Domínguez C, Fachal C, Alvarez M. Navarro C, et al. Among authors: fernandez jm. Neurology. 1996 Jan;46(1):254-6. doi: 10.1212/wnl.46.1.254. Neurology. 1996. PMID: 8559389

6

Adult glycogenosis II with paracrystalline mitochondrial inclusions and Hirano bodies in skeletal muscle.

Fernández R, Fernández JM, Cervera C, Teijeira S, Teijeiro A, Domínguez C, Navarro C. Fernández R, et al. Among authors: fernandez jm. Neuromuscul Disord. 1999 May;9(3):136-43. doi: 10.1016/s0960-8966(98)00117-5. Neuromuscul Disord. 1999. PMID: 10382906

7

Autosomal dominant limb-girdle muscular dystrophy: a large kindred with evidence for anticipation.

Gamez J, Navarro C, Andreu AL, Fernandez JM, Palenzuela L, Tejeira S, Fernandez-Hojas R, Schwartz S, Karadimas C, DiMauro S, Hirano M, Cervera C. Gamez J, et al. Among authors: fernandez hojas r, fernandez jm. Neurology. 2001 Feb 27;56(4):450-4. doi: 10.1212/wnl.56.4.450. Neurology. 2001. PMID: 11222786

8

Fabry disease: an ultrastructural comparative study of skin in hemizygous and heterozygous patients.

Navarro C, Teijeira S, Dominguez C, Fernandez JM, Rivas E, Fachal C, Barrera S, Rodriguez C, Iranzo P. Navarro C, et al. Among authors: fernandez jm. Acta Neuropathol. 2006 Feb;111(2):178-85. doi: 10.1007/s00401-005-0026-8. Epub 2006 Feb 7. Acta Neuropathol. 2006. PMID: 16463201

9

Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large family.

Sobrido MJ, Fernández JM, Fontoira E, Pérez-Sousa C, Cabello A, Castro M, Teijeira S, Alvarez S, Mederer S, Rivas E, Seijo-Martínez M, Navarro C. Sobrido MJ, et al. Among authors: fernandez jm. Brain. 2005 Jul;128(Pt 7):1716-27. doi: 10.1093/brain/awh511. Epub 2005 Apr 27. Brain. 2005. PMID: 15857933

10

Case report: four-year follow-up of bone-marrow transplantation in late juvenile metachromatic leukodystrophy.

Navarro C, Domínguez C, Fernández JM, Fachal C, Alvárez M. Navarro C, et al. Among authors: fernandez jm. J Inherit Metab Dis. 1995;18(2):157-8. doi: 10.1007/BF00711754. J Inherit Metab Dis. 1995. PMID: 7564234 No abstract available.

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